Evidence map›Paper›PMID 36596941›Full record

ArticlePediatric research2023

The role of vitamin D receptor gene polymorphism in the development of necrotizing enterocolitis.

Dogan Barut, Mete Akisu, Ozge Altun Koroglu, Demet Terek, Firat Ergin, Huseyin Onay, Mehmet Yalaz, Nilgun Kultursay

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 36% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Dogan BarutDepartment of Pediatrics, Ege University Hospital, Bornova, Izmir, 35100, Turkey. barutd047@gmail.com.
Mete AkisuDepartment of Pediatrics, Division of Neonatology, Ege University Hospital, Bornova, Izmir, 35100, Turkey.
Ozge Altun KorogluDepartment of Pediatrics, Division of Neonatology, Ege University Hospital, Bornova, Izmir, 35100, Turkey.
Demet TerekDepartment of Pediatrics, Division of Neonatology, Ege University Hospital, Bornova, Izmir, 35100, Turkey.
Firat ErginDepartment of Pediatrics, Division of Neonatology, Ege University Hospital, Bornova, Izmir, 35100, Turkey.
Huseyin OnayDepartment of Medical Genetics, Ege University Hospital, Bornova, Izmir, 35100, Turkey.
Mehmet YalazDepartment of Pediatrics, Division of Neonatology, Ege University Hospital, Bornova, Izmir, 35100, Turkey.
Nilgun KultursayDepartment of Pediatrics, Division of Neonatology, Ege University Hospital, Bornova, Izmir, 35100, Turkey.
Ege University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVitamin D and its receptor (VDR) effects on the gastrointestinal system are among its most critical multisystemic effects.

methodsThis study aimed to reveal that VDR gene polymorphisms may constitute a risk factor for necrotizing enterocolitis (NEC). VDR Fok1-Bsm1-Apa single-nucleotide polymorphisms were analyzed in the NEC group (n = 74) and the control group (n = 147). Among 1112 babies at and below 36 weeks of gestational age who were hospitalized between January 2013 and December 2016 with a diagnosis of prematurity, 74 of a total of 148 patients who developed NEC during follow-up (NEC group) were included in the study. When NEC was diagnosed according to clinical and radiological findings and staged using Modified Bell criteria, 9 (12.1%) of 74 babies were stage 1A, 13 (17.5%) stage 1B, and 5 (6.7%) stage 2A, 33 (44.5%) stage 2B, 7 (9.4%) stage 3A, 7 (9.4%) stage 3B. Of 964 babies who did not develop NEC during follow-up, 147 were included as the control group in the study. Genotyping of VDR polymorphisms was assayed by real-time PCR. From 221 premature babies in the NEC and control groups, 2 ml peripheral blood was taken appropriately and meticulously into an EDTA tube. DNA was isolated from these blood samples. DNA amplification was performed using a thermal cycler (Applied Biosystems GeneAmp PCR System 9600).

resultsWhen the two groups were compared in terms of the prevalence of VDR Fok1 C/T genotype, it was found that TT genotype increased the risk of NEC by 2.697 times, and there was a significant relationship between TT genotype and the risk of NEC (p = 0.041). Multivariable logistic regression analysis was performed in terms of gestational age, birth weight, VDR gene polymorphism data between NEC and the control group. According to the analysis results, TT polymorphism, increased the risk of disease 4.5 times (p = 0.033).

conclusionFok 1 C > T polymorphism in the VDR gene plays a role in the development of NEC. Identifying the risk groups by detecting gene polymorphisms that cause increased susceptibility to NEC may assist in the follow-up of these patients and in making early treatment decisions for them. IMPACT: In this study examining the non-bone effects of the genetic differences in vitamin D metabolism in premature babies, Fok 1 polymorphism has been observed to be an essential risk factor for NEC. This is the first study in our country that has investigated the relationship between VDR gene polymorphism and necrotizing enterocolitis among the Turkish population. Identifying the risk groups by detecting gene polymorphisms that cause increased susceptibility to NEC may assist in the monitoring of these patients and in making early treatment decisions for them.

Indexed as

Enterocolitis, NecrotizingFetal DiseasesInfant, Newborn, DiseasesFemaleGenetic Predisposition to DiseaseGenotypeHumansInfant, NewbornPolymorphism, Single NucleotideReal-Time Polymerase Chain ReactionReceptors, CalcitriolVitamin DReceptors, CalcitriolVitamin D

Identifiers

PMID36596941
OpenAlexW4313488095

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.